173 results on '"Fiuza-Luces C"'
Search Results
2. Assessment of resting energy expenditure in pediatric mitochondrial diseases with indirect calorimetry
- Author
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Fiuza-Luces, C., Santos-Lozano, A., García-Silva, M.T., Martín-Hernández, E., Quijada-Fraile, P., Marín-Peiró, M., Campos, P., Arenas, J., Lucía, A., Martín, M.A., and Morán, M.
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- 2016
- Full Text
- View/download PDF
3. Response rate to the treatment of Waldenström macroglobulinemia: A meta-analysis of the results of clinical trials
- Author
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Santos-Lozano, A., Morales-Gonzalez, A., Sanchis-Gomar, F., Cristi-Montero, C., Fiuza-Luces, C., Pareja-Galeano, H., Martínez-López, J., Garatachea, N., and Lucia, A.
- Published
- 2016
- Full Text
- View/download PDF
4. Effects of allopurinol on exercise-induced muscle damage: new therapeutic approaches?
- Author
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Sanchis-Gomar, F., Pareja-Galeano, H., Perez-Quilis, C., Santos-Lozano, A., Fiuza-Luces, C., Garatachea, N., Lippi, G., and Lucia, A.
- Published
- 2015
5. Physical function and quality of life in patients with chronic GvHD: a summary of preclinical and clinical studies and a call for exercise intervention trials in patients
- Author
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Fiuza-Luces, C, Simpson, R J, Ramírez, M, Lucia, A, and Berger, N A
- Published
- 2016
- Full Text
- View/download PDF
6. Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?
- Author
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Instituto de Salud Carlos III, European Commission, Consejo Nacional de Ciencia y Tecnología (México), Villarreal-Salazar, M., Santalla, A., Real-Martínez, A., Nogales-Gadea, G., Valenzuela, P. L., Fiuza-Luces, C., Andreu, Antoni L., Rodríguez-Aguilera, Juan Carlos, Martín, Miguel A., Arenas, Joaquín, Vissing, J., Lucía, A., Krag, T. O., Pinós, T., Instituto de Salud Carlos III, European Commission, Consejo Nacional de Ciencia y Tecnología (México), Villarreal-Salazar, M., Santalla, A., Real-Martínez, A., Nogales-Gadea, G., Valenzuela, P. L., Fiuza-Luces, C., Andreu, Antoni L., Rodríguez-Aguilera, Juan Carlos, Martín, Miguel A., Arenas, Joaquín, Vissing, J., Lucía, A., Krag, T. O., and Pinós, T.
- Abstract
[Background]: McArdle disease is caused by myophosphorylase deficiency and results in complete inability for muscle glycogen breakdown. A hallmark of this condition is muscle oxidation impairment (e.g., low peak oxygen uptake (VO2peak)), a phenomenon traditionally attributed to reduced glycolytic flux and Krebs cycle anaplerosis. Here we hypothesized an additional role for muscle mitochondrial network alterations associated with massive intracellular glycogen accumulation. [Methods]: We analyzed in depth mitochondrial characteristics-content, biogenesis, ultrastructure-and network integrity in skeletal-muscle from McArdle/control mice and two patients. We also determined VO2peak in patients (both sexes, N = 145) and healthy controls (N = 133). [Results]: Besides corroborating very poor VO2peak values in patients and impairment in muscle glycolytic flux, we found that, in McArdle muscle: (a) damaged fibers are likely those with a higher mitochondrial and glycogen content, which show major disruption of the three main cytoskeleton components-actin microfilaments, microtubules and intermediate filaments-thereby contributing to mitochondrial network disruption in skeletal muscle fibers; (b) there was an altered subcellular localization of mitochondrial fission/fusion proteins and of the sarcoplasmic reticulum protein calsequestrin-with subsequent alteration in mitochondrial dynamics/function; impairment in mitochondrial content/biogenesis; and (c) several OXPHOS-related complex proteins/activities were also affected. [Conclusions]: In McArdle disease, severe muscle oxidative capacity impairment could also be explained by a disruption of the mitochondrial network, at least in those fibers with a higher capacity for glycogen accumulation. Our findings might pave the way for future research addressing the potential involvement of mitochondrial network alterations in the pathophysiology of other glycogenoses.
- Published
- 2022
7. Low aerobic capacity in McArdle disease:A role for mitochondrial network impairment?
- Author
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Villarreal-Salazar, M., Santalla, A., Real-Martínez, A., Nogales-Gadea, G., Valenzuela, P. L., Fiuza-Luces, C., Andreu, A. L., Rodríguez-Aguilera, J. C., Martín, M. A., Arenas, J., Vissing, J., Lucia, A., Krag, T. O., Pinós, T., Villarreal-Salazar, M., Santalla, A., Real-Martínez, A., Nogales-Gadea, G., Valenzuela, P. L., Fiuza-Luces, C., Andreu, A. L., Rodríguez-Aguilera, J. C., Martín, M. A., Arenas, J., Vissing, J., Lucia, A., Krag, T. O., and Pinós, T.
- Abstract
Background: McArdle disease is caused by myophosphorylase deficiency and results in complete inability for muscle glycogen breakdown. A hallmark of this condition is muscle oxidation impairment (e.g., low peak oxygen uptake (VO2peak)), a phenomenon traditionally attributed to reduced glycolytic flux and Krebs cycle anaplerosis. Here we hypothesized an additional role for muscle mitochondrial network alterations associated with massive intracellular glycogen accumulation. Methods: We analyzed in depth mitochondrial characteristics-content, biogenesis, ultrastructure-and network integrity in skeletal-muscle from McArdle/control mice and two patients. We also determined VO2peak in patients (both sexes, N = 145) and healthy controls (N = 133). Results: Besides corroborating very poor VO2peak values in patients and impairment in muscle glycolytic flux, we found that, in McArdle muscle: (a) damaged fibers are likely those with a higher mitochondrial and glycogen content, which show major disruption of the three main cytoskeleton components-actin microfilaments, microtubules and intermediate filaments-thereby contributing to mitochondrial network disruption in skeletal muscle fibers; (b) there was an altered subcellular localization of mitochondrial fission/fusion proteins and of the sarcoplasmic reticulum protein calsequestrin-with subsequent alteration in mitochondrial dynamics/function; impairment in mitochondrial content/biogenesis; and (c) several OXPHOS-related complex proteins/activities were also affected. Conclusions: In McArdle disease, severe muscle oxidative capacity impairment could also be explained by a disruption of the mitochondrial network, at least in those fibers with a higher capacity for glycogen accumulation. Our findings might pave the way for future research addressing the potential involvement of mitochondrial network alterations in the pathophysiology of other glycogenoses.
- Published
- 2022
8. Benefits of exercise and immunotherapy in a murine model of human non-small-cell lung carcinoma.
- Author
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Martin-Ruiz, A, Fiuza-Luces, C, Rincón-Castanedo, C, Fernández-Moreno, D, González Gálvez, Beatriz, Martínez-Martínez, E, Martín-Acosta, P, Coronado, MJ, Franco-Luzón, L, González-Murillo, A, Ramírez, M, Provencio, M, Lucia, A, Martin-Ruiz, A, Fiuza-Luces, C, Rincón-Castanedo, C, Fernández-Moreno, D, González Gálvez, Beatriz, Martínez-Martínez, E, Martín-Acosta, P, Coronado, MJ, Franco-Luzón, L, González-Murillo, A, Ramírez, M, Provencio, M, and Lucia, A
- Abstract
Background: Lung cancer has the highest incidence and mortality rate in the world. One of the most promising new cancer therapies in recent years is immunotherapy, which is based on the blockade of immune checkpoints such as programmed cell death protein 1 (PD-1). Exercise training is beneficial to maintain and improve the quality of life of cancer patients, and it might also modulate the anti-tumoral efficiency of some chemotherapeutic agents. However, the potential of exercise combined with immunotherapy as a cancer therapy remains to be elucidated. Here, we examined the effects of exercise on tumor growth and its possible adjuvant effects when combined with anti-PD-1 immunotherapy (nivolumab) in a patient derived xenograft (PDX) model of non-small-cell lung carcinoma (NSCLC). Methods: We generated a PDX model using NOD-SCID gamma mice with subcutaneous grafts from tumor tissue of a patient with NSCLC. Animals were randomly assigned to one of four groups: non-exercise + isotype control (n=5), exercise + isotype control (n=5), non-exercise + nivolumab (n=6) or exercise + nivolumab (n=6). The animals undertook an 8- week moderate-intensity training regimen (treadmill aerobic exercise and strength training). Immunotherapy (nivolumab) or an isotype control was administered 2 days/week, for 6 weeks. Several tumor growth and microenvironment parameters were measured after the intervention. Results: Improvements in aerobic capacity and muscle strength (p=0.027 and p=0.005) were noted in exercised animals. Exercise alone reduced the tumor growth rate with respect to non-exercised mice (p=0.050). The double intervention (exercise + nivolumab) increased tumor necrosis and reduced apoptosis with respect to controls (p=0.026; p=0.030). All interventions achieved a reduction in proliferation compared with the control group (p=0.015, p=0.011, and p=0.011). Exercise alone increased myeloid tumor infiltrates (mostly neutrophils) with respect to the nivolumab only group (p=0.018)., Ministerio de Economía y Competitividad (España), National Strength and Conditioning Association, European Commission, Depto. de Bioquímica y Biología Molecular, TRUE, pub
- Published
- 2020
9. ACTN3 genotype in Spanish elite swimmers: No “heterozygous advantage”
- Author
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Ruiz, J. R., Santiago, C., Yvert, T., Muniesa, C., Díaz-Ureña, G, Bekendam, N., Fiuza-Luces, C., Gómez-Gallego, F, Femia, P., and Lucia, A.
- Published
- 2013
- Full Text
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10. Effects of Exercise on the Immune Function of Pediatric Patients With Solid Tumors Insights From the PAPEC Randomized Trial
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Fiuza-Luces C, Padilla J, Valentin J, Santana-Sosa E, Santos-Lozano A, Sanchis-Gomar F, Pareja-Galeano H, Morales J, Fleck S, Perez M, Lassaletta A, Soares-Miranda L, Perez-Martinez A, and Lucia A
- Subjects
Immunology ,Cytokines ,Physical Activity ,Cancer - Abstract
The purpose of this study was to assess the effects of an in-hospital exercise intervention during neoadjuvant chemotherapy on the inflammatory profile and immune cell subpopulation in 20 children with solid tumors (control [n = 11] and exercise group [ n = 9]). Although no significant interaction (group x time) effect was found with an analysis of variance test, we found a trend toward an interaction effect for natural killer cells expressing the immunoglobulin-like receptor KIR2DS4, with their numbers remaining stable in the exercise group but increasing in controls. Our data support that exercise interventions are safe in pediatric cancer patients with solid tumors during chemotherapy treatment despite its aggressive, immunosuppressive nature.
- Published
- 2017
11. Benefits of skeletal-muscle exercise training in pulmonary arterial hypertension: The WHOLEi+12 trial
- Author
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Gonzalez-Saiz L, Fiuza-Luces C, Sanchis-Gomar F, Santos-Lozano A, Quezada-Loaiza C, Flox-Camacho A, Munguia-Izquierdo D, Ara I, Santalla A, Moran M, Sanz-Ayan P, Escribano-Subias P, and Lucia A
- Subjects
VO2peak ,NT-proBNP ,Pulmonary disease ,Resistance exercise ,Cardio-pulmonary exercise testing - Abstract
Background: Pulmonary arterial hypertension is often associated with skeletal-muscle weakness. The purpose of this randomized controlled trial was to determine the effects of an 8-week intervention combining muscle resistance, aerobic and inspiratory pressure-load exercises on upper/lower-body muscle power and other functional variables in patients with this disease. Methods: Participants were allocated to a control (standard care) or intervention (exercise) group (n = 20 each, 45 +/- 12 and 46 +/- 11 years, 60% women and 10% patients with chronic thromboembolic pulmonary hypertension per group). The intervention included five, three and six supervised (inhospital) sessions/week of aerobic, resistance and inspiratory muscle training, respectively. The primary endpoint was peak muscle power during bench/leg press; secondary outcomes included N-terminal pro-brain natriuretic peptide levels, 6-min walking distance, five-repetition sit-to-stand test, maximal inspiratory pressure, cardiopulmonary exercise testing variables (e.g., peak oxygen uptake), health-related quality of life, physical activity levels, and safety. Results: Adherence to training sessions averaged 94 +/- 0.5% (aerobic), 98 +/- 0.3% (resistance) and 91 +/- 1% (inspiratory training). Analysis of variance showed a significant interaction (group x time) effect for leg/bench press (P < 0.001/P = 0.002), with both tests showing an improvement in the exercise group (P < 0.001) but not in controls (P > 0.1). We found a significant interaction effect (P < 0.001) for five-repetition sit-to-stand test, maximal inspiratory pressure and peak oxygen uptake (P < 0.001), indicating a training-induced improvement. No major adverse event was noted due to exercise. Conclusions: An 8-week exercise intervention including aerobic, resistance and specific inspiratory muscle training is safe for patients with pulmonary arterial hypertension and yields significant improvements in muscle power and other functional variables. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
- Published
- 2017
12. Ideal cardiovascular health (ICVH) in patients with a recent diagnosis of colorectal cancer (CRC)
- Author
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Ramos, J., primary, Álvarez-Bustos, A., additional, Soriano, M., additional, Nuñez, B., additional, Ros, J., additional, Osorio, P., additional, Gutierrez, L., additional, Gómez, R., additional, Hidalgo, F., additional, Leon, A., additional, Mendez, M., additional, González, C., additional, Sanchez, A., additional, Martínez, S., additional, Pagola, I., additional, Brea, L., additional, Fiuza-Luces, C., additional, Lucia, A., additional, and Ruiz-Casado, A., additional
- Published
- 2017
- Full Text
- View/download PDF
13. Variaciones genéticas en la vía de la mitocondriogénesis PPARD-PPARGC1A-NRF-TFAM no están asociadas ni con características musculares ni con rendimiento físico en personas mayores
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Garatachea-Vallejo, N., Santiago, C., Yvert, T., Verde-Rello, Z., Fiuza-Luces, C., Santos-Lozano, A., Gómez-Gallego, F., and Lucía, A.
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Polimorfismo genético ,Genética humana ,human activities - Abstract
We studied the influence of genetic polymorphisms involved in the PPARD-PPARGC1A-NRF-TFAM mitochondriogenesis pathway (rs6949152, rs12594956, rs2267668, rs8192678, and rs1937) on muscle phenotypes (thigh muscles’ cross-sectional, maximal handgrip-strength and 30-second chair stand-test) and Barthel index in Caucasian (Spanish) community-dwelling old people (n=75, 21 men, 54 women; 71–94 years). We found no significant genetic associations with the studied phenotypes. Multiple, complex gene-environment and gene-gene interactions which are yet to be determined are likely to play a more determinant role. Se estudió la influencia de los polimorfismos genéticos implicados en la vía de mitocondriogénesis PPARD-PPARGC1A-NRF-TFAM (rs6949152, rs12594956, rs2267668, rs8192678 y rs1937) en distintos fenotipos musculares (sección transversal muscular del muslo, fuerza máxima de prensión manual y 30 segundos de sentarse-levantarse de una silla) y en el índice de Barthel en personas mayores caucásicas (españoles) (n = 75, 21 hombres, 54 mujeres; 71 a 94 años). No se encontraron asociaciones genéticas significativas con los fenotipos estudiados. Interacciones múltiples, complejos gen-ambiente y relaciones gen-gen aún no determinadas podrían desempeñar un papel más determinante. Fondo de Investigaciones Sanitarias (FIS, grant # PI09-00194). 0.225 SJR (2015) Q3, 107/167 Physical therapy, sports therapy and rehabilitation; Q4, 107/128 Sports science UEM
- Published
- 2015
14. MSTN K153R polymorphism as candidate gene to influence extreme longevity in spanish centenarian women
- Author
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Garatachea, N., Rodríguez-Romo, G., Santos-Lozano, A., Santiago-Dorrego, C., Yvert, T., Fiuza-Luces, C., and Lucia, A.
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Genética - Abstract
El gen de la miostatina (MSTN) es uno de los genes candidatos que podría influir en la longevidad extrema, debido a su papel en la modulación de masa muscular y sarcopenia, además de su papel en la inhibición de la principal vía de señalización de nutrientes relacionada con la longevidad, mTOR (del inglés, ‘mammalian target-of-rapamycin’). Comparamos la distribución alélica/genotípica de las variantes exónicas de la MSTN K153R (rs1805086), E164K (rs35781413), I225T y P198A, en centenarias (casos, n=132; rango edad: 100-107) y mujeres jóvenes (controles, n=167, < 50 años). La frecuencia de la variante alélica R y de los portadores de este la misma (genotipos KR o RR) fue significativamente superior en centenarias (6.8% y 12.1%) que en controles (1.5% y 3.8%) (p=0.0008 y p=0.0022 respectivamente). La razón de verosimilitud (‘odds ratio’, abreviado ‘OR’) de ser un centenaria si el sujeto tiene un alelo-R fue 4.47 (con un intervalo de confianza del 95% (CI): 1.59-12.54; p=0.004), comparado con el grupo control. Aunque son necesarias nuevas investigaciones, el alelo variante R del polimorfismo MSTN K153R podría ser uno de los contribuidores genéticos asociados con excepcional longevidad. The myostatin (MSTN) gene is a candidate to influence extreme longevity owing to its role in modulating muscle mass and sarcopenia, and especially in inhibiting the main nutrient-sensing pathway involved in longevity, i.e. mTOR (mammalian target-of-rapamycin). We compared allele/genotype distributions of the exonic MSTN variants K153R (rs1805086), E164K (rs35781413), I225T and P198A, in women centenarians (cases, n=132; age range: 100-107 years) and younger women adults (controls, n=167; age < 50 years). The frequency of the variant R-allele and of R-allele carriers was significantly higher in centenarians (6.8% and 12.1%) than in controls (1.5% and 3.8%) (p=0.0008 and p=0.0022 respectively). The odds ratio (OR) of being a centenarian if the subject had the R allele was 4.47 (95% confidence interval (CI): 1.59-12.54 p=0.004), compared to the control group. Although more research is needed, the variant allele of the MSTN K153R polymorphism could be among the genetic contributors associated with exceptional longevity. Sin financiación No data 2014 UEM
- Published
- 2014
15. Cancer-related fatigue in breast cancer survivors: more evidence for a physiological substrate
- Author
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Ramos, J., primary, Cantos, B., additional, Maximiano, C., additional, Cebolla, H., additional, Fiuza-Luces, C., additional, Gutierrez, L., additional, Osorio, P., additional, Cerrato, J., additional, Sanchez, J.L., additional, Nuñez, B., additional, Garate, A., additional, Pagola, I., additional, Alejo, L.B., additional, Lucia, A., additional, and Ruiz-Casado, A., additional
- Published
- 2016
- Full Text
- View/download PDF
16. Exercise intervention in a family with exercise intolerance and a novel mutation in the mitochondrial POLG gene
- Author
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Morán, M., primary, Blázquez, A., additional, Fiuza-Luces, C., additional, Díez-Bermejo, J., additional, Delmiro, A., additional, Docampo, J., additional, Serrano-Lorenzo, P., additional, González-Quintana, A., additional, Arenas, J., additional, Laín-Hernández, A., additional, Lucía, A., additional, Domínguez-González, C., additional, and Martín, M., additional
- Published
- 2016
- Full Text
- View/download PDF
17. Validity of the Physical Activity Questionnaires IPAQ-SF and GPAQ for Cancer Survivors: Insights from a Spanish Cohort
- Author
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Ruiz-Casado, A., additional, Alejo, L., additional, Santos-Lozano, A., additional, Soria, A., additional, Ortega, M., additional, Pagola, I., additional, Fiuza-Luces, C., additional, Palomo, I., additional, Garatachea, N., additional, Cebolla, H., additional, and Lucia, A., additional
- Published
- 2016
- Full Text
- View/download PDF
18. Physical function and quality of life in patients with chronic GvHD: a summary of preclinical and clinical studies and a call for exercise intervention trials in patients
- Author
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Fiuza-Luces, C, primary, Simpson, R J, additional, Ramírez, M, additional, Lucia, A, additional, and Berger, N A, additional
- Published
- 2015
- Full Text
- View/download PDF
19. 1601P - Ideal cardiovascular health (ICVH) in patients with a recent diagnosis of colorectal cancer (CRC)
- Author
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Ramos, J., Álvarez-Bustos, A., Soriano, M., Nuñez, B., Ros, J., Osorio, P., Gutierrez, L., Gómez, R., Hidalgo, F., Leon, A., Mendez, M., González, C., Sanchez, A., Martínez, S., Pagola, I., Brea, L., Fiuza-Luces, C., Lucia, A., and Ruiz-Casado, A.
- Published
- 2017
- Full Text
- View/download PDF
20. Resistance Training Does not have an Effect on Cognition or Related Serum Biomarkers in Nonagenarians: A Randomized Controlled Trial
- Author
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Ruiz, J., additional, Gil-Bea, F., additional, Bustamante-Ara, N., additional, Rodríguez-Romo, G., additional, Fiuza-Luces, C., additional, Serra-Rexach, J., additional, Cedazo-Minguez, A., additional, and Lucia, A., additional
- Published
- 2014
- Full Text
- View/download PDF
21. Effects of allopurinol on exercise-induced muscle damage: new therapeutic approaches?
- Author
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Sanchis-Gomar, F., primary, Pareja-Galeano, H., additional, Perez-Quilis, C., additional, Santos-Lozano, A., additional, Fiuza-Luces, C., additional, Garatachea, N., additional, Lippi, G., additional, and Lucia, A., additional
- Published
- 2014
- Full Text
- View/download PDF
22. P.291 - Exercise intervention in a family with exercise intolerance and a novel mutation in the mitochondrial POLG gene
- Author
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Morán, M., Blázquez, A., Fiuza-Luces, C., Díez-Bermejo, J., Delmiro, A., Docampo, J., Serrano-Lorenzo, P., González-Quintana, A., Arenas, J., Laín-Hernández, A., Lucía, A., Domínguez-González, C., and Martín, M.
- Published
- 2016
- Full Text
- View/download PDF
23. 1496P - Cancer-related fatigue in breast cancer survivors: more evidence for a physiological substrate
- Author
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Ramos, J., Cantos, B., Maximiano, C., Cebolla, H., Fiuza-Luces, C., Gutierrez, L., Osorio, P., Cerrato, J., Sanchez, J.L., Nuñez, B., Garate, A., Pagola, I., Alejo, L.B., Lucia, A., and Ruiz-Casado, A.
- Published
- 2016
- Full Text
- View/download PDF
24. Validity of the Physical Activity Questionnaires IPAQSF and GPAQ for Cancer Survivors: Insights from a Spanish Cohort.
- Author
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Ruiz-Casado, A., Alejo, L. B., Santos-Lozano, A., Soria, A., Ortega, M. J., Pagola, I., Fiuza-Luces, C., Palomo, I., Garatachea, N., Cebolla, H., and Lucia, A.
- Subjects
CANCER patients ,CHI-squared test ,CONFIDENCE intervals ,STATISTICAL correlation ,RESEARCH methodology ,PROBABILITY theory ,QUESTIONNAIRES ,STATISTICS ,DATA analysis ,ACCELEROMETRY ,CROSS-sectional method ,RECEIVER operating characteristic curves ,RESEARCH methodology evaluation ,PHYSICAL activity ,DATA analysis software - Abstract
Regular physical activity (PA) decreases mortality risk in survivors of breast and colorectal cancer. Such impacts of exercise have prompted initiatives designed both to promote and adequately monitor PA in cancer survivors. This study examines the validity of 2 widely used selfreport methods for PA determination, the International Physical Activity Questionnaire short version (IPAQ-SF) and Global Physical Activity Questionnaire (GPAQ). Both instruments were compared with the triaxial accelerometry (Actigraph) method as an objective reference standard. Study participants were 204 cancer survivors (both sexes, aged 18-79 years). Compared with accelerometry, both questionnaires significantly overestimated PA levels (across all intensities) and underestimated physical inactivity levels. No differences were detected between the 2 questionnaires except for a shorter inactivity time estimated by GPAQ (p = 0.001). The Bland and Altman method confirmed that both questionnaires overestimated all PA levels. Receiver operating characteristic (ROC) analysis classified IPAQ and GPAQ as fair and poor predictors, respectively, of the proportions of survivors fulfilling international PA recommendations ( ≥ 150 min ⋅ week
-1 of moderate-vigorous PA). IPAQ-SF showed a higher sensitivity but lower specificity than GPAQ. Our data do not support the use of IPAQ-SF or GPAQ to determine PA or inactivity levels in cancer survivors. [ABSTRACT FROM AUTHOR]- Published
- 2016
- Full Text
- View/download PDF
25. Exercise Training and Cytokines in Breast Cancer Survivors
- Author
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Gómez, A. M., primary, Martínez, C., additional, Fiuza-Luces, C., additional, Herrero, F., additional, Pérez, M., additional, Madero, L., additional, Ruiz, J. R., additional, Lucia, A., additional, and Ramírez, M., additional
- Published
- 2011
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26. GNB3C825T Polymorphism and Elite Athletic Status: A Replication Study with Two Ethnic Groups
- Author
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Ruiz, J. R., primary, Eynon, N., additional, Meckel, Y., additional, Fiuza-Luces, C., additional, Santiago, C., additional, Gómez-Gallego, F., additional, Oliveira, J., additional, and Lucia, A., additional
- Published
- 2010
- Full Text
- View/download PDF
27. Resistance Training Does not have an Effect on Cognition or Related Serum Biomarkers in Nonagenarians: A Randomized Controlled Trial.
- Author
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Ruiz, J. R., Gil-Bea, F., Bustamante-Ara, N., Rodríguez-Romo, G., Fiuza-Luces, C., Serra-Rexach, J. A., Cedazo-Minguez, A., and Lucia, A.
- Subjects
AGE distribution ,AGING ,ANALYSIS of covariance ,BIOMARKERS ,BODY weight ,COGNITION ,EXERCISE ,PROTEINS ,PULMONARY function tests ,STATISTICAL sampling ,TUMOR necrosis factors ,DATA analysis ,PHYSICAL training & conditioning ,BODY mass index ,RANDOMIZED controlled trials ,CONTROL groups ,DATA analysis software - Abstract
The aim of this randomized controlled trial was to determine the effects of 8-week exercise-intervention on cognition and related serum biochemical markers in nonagenarians. We also studied the effects of a 4-week training cessation ('detraining') period on our study variables. Participants were randomly allocated to a standard-care (control) or intervention (exercise) group [n=20 (16 women)/group]. The intervention focused on supervised, light-to-moderate-intensity aerobic and resistance exercises (mainly leg press), and included 3 weekly sessions. Cognitive status was determined by the mini-mental state examination and geriatric depression scale. We analysed proteins with reported relation with mechanisms behind cognition changes such as serum levels of angiotensin converting enzyme, amyloid-precursor protein, epidermal growth factor, brain-derived neural factor and tumor necrosis factor. No significant change (P>0.05) in any of the variables studied was found following the exercise intervention compared with the standard-care group. Similarly, no significant changes (P>0.05) were observed following the detraining period compared with the standard-care group. Overall changes after the exercise intervention in serum biomarkers were not associated with changes in functional capacity and cognitive measures. An 8-week exercise intervention focusing on resistance exercises neither benefits cognitive function nor affects the levels of the serum proteins analysed in nonagenarians. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
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28. GNB3 C825T Polymorphism and Elite Athletic Status: A Replication Study with Two Ethnic Groups.
- Author
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Ruiz, J. R., Eynon, N., Meckel, Y., Fiuza-Luces, C., Santiago, C., Gómez-Gallego, F., Oliveira, J., and Lucia, A.
- Abstract
We aimed to replicate the original findings by Eynon etal. [4] showing an association between the T alíele of the CNB3 C825T polymorphism and elite endurance athletic status, in larger cohorts and in other ethnicities. We compared allelic and genotypic frequencies of the CNB3 C825T polymorphism among non-athletic controls (N=340), elite endurance athletes (N = 174), and power athletes (N = 134). The population sample included participants from 2 different ethnic/geographic backgrounds (Israel and Spain). We observed no significant differences in genotypic and allelic frequencies between countries or groups (all P>0.1). The odds ratio (OR) of being an endurance athlete if the subject had a T alíele was 0.841 (95%CI: 0.638-1.110) compared to the control group and 1.047 (95% CI: 0.751-1.461) compared to the power group. Our findings support the need to corroborate genotype :phenotype associations in the field of sports genetics with the largest possible population samples, including populations of different ethnic backgrounds. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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29. Baicalin supplementation reduces serum biomarkers of skeletal muscle wasting and may protect against lean body mass reduction in cancer patients: Results from a pilot open-label study
- Author
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Emanuele, E., Bertona, M., Pareja-Galeano, H., Fiuza-Luces, C., Morales, J. S., Sanchis-Gomar, F., and Alejandro Lucia
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Enfermos de cáncer ,Salud ,Cáncer ,Oncología - Abstract
Muscle wasting in patients with cancer has been linked to an increased activity of nuclear factor κB (NF-κB) and higher circulating levels of activin-A (ActA), a negative growth factor for muscle mass. Baicalin is a natural flavonoid that can reduce skeletal muscle atrophy in animal models of cancer cachexia by inhibiting NF-κB. This pilot open-label study assessed the effects of baicalin supplementation (50 mg daily for 3 months) in cancer patients who showed involuntary weight loss >5% over the past 6 months. A total of 20 patients were investigated. Participants were evaluated at baseline and at the end of the 3-month study period for the following endpoints: 1) changes from baseline in serum NF-κB and ActA levels; and 2) change from baseline in lean body mass (LBM). We observed significant reduction in both NF-κB (p
30. ACTN3 R577X polymorphism in marathon athletes
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Garatachea, N., Fiuza-Luces, C., Marín, M., Reyes, A., Alejandro Santos-Lozano, and Lucía, A.
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Ciencia ,Maratón - Atletismo ,Deporte ,Genética humana ,Ejercicio ,Genética - Abstract
The effect of ACTN3 has mainly been studied in elite athletes, bades on the hypothesis that its influence on muscle function would be most readily observable at the extremes of human performance. The main purpose of this study was to examine the association of ACTN3 with marathon performance across a wide range of competition levels. 0.146 SJR (2014) Q4, 199/231 Health (social science), 131/169 Physical therapy, sports therapy and rehabilitation, 119/128 Sports sciences UEM
31. Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?
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M. Villarreal-Salazar, A. Santalla, A. Real-Martínez, G. Nogales-Gadea, P.L. Valenzuela, C. Fiuza-Luces, A.L. Andreu, J.C. Rodríguez-Aguilera, M.A. Martín, J. Arenas, J. Vissing, A. Lucia, T.O. Krag, T. Pinós, Instituto de Salud Carlos III, European Commission, Consejo Nacional de Ciencia y Tecnología (México), Institut Català de la Salut, [Villarreal-Salazar M, Real-Martínez A, Pinós T] Grup de Recerca de Patologia Neuromuscular i Mitocondrial, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Santalla A] Universidad Pablo de Olavide, Sevilla, Spain. [Nogales-Gadea G] Grup de Recerca en Malalties Neuromusculars i Neuropediàtriques, Department of Neurosciences, Institut d’Investigacio en Ciencies de la Salut Germans Trias i Pujol i Campus Can Ruti, Universitat Autònoma de Barcelona, Badalona, Spain. [Valenzuela PL, Fiuza-Luces C] Physical Activity and Health Research Group (‘PaHerg’), Research Institute of the Hospital 12 de Octubre (‘imas12’), Madrid, Spain, and Vall d'Hebron Barcelona Hospital Campus
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fenómenos fisiológicos nerviosos y musculoesqueléticos::fenómenos fisiológicos musculoesqueléticos::resistencia física::tolerancia al ejercicio [FENÓMENOS Y PROCESOS] ,McArdle disease ,células::estructuras celulares::espacio intracelular::citoplasma::estructuras citoplasmáticas::orgánulos::mitocondrias [ANATOMÍA] ,enfermedades nutricionales y metabólicas::enfermedades metabólicas::alteraciones congénitas del metabolismo::trastornos congénitos del metabolismo de los carbohidratos::enfermedad por almacenamiento de glucógeno::enfermedad por almacenamiento de glucógeno tipo V [ENFERMEDADES] ,Skeletal muscle ,Exercici ,Cell Biology ,Musculoskeletal and Neural Physiological Phenomena::Musculoskeletal Physiological Phenomena::Physical Endurance::Exercise Tolerance [PHENOMENA AND PROCESSES] ,Nutritional and Metabolic Diseases::Metabolic Diseases::Metabolism, Inborn Errors::Carbohydrate Metabolism, Inborn Errors::Glycogen Storage Disease::Glycogen Storage Disease Type V [DISEASES] ,Aerobic capacity ,Cells::Cellular Structures::Intracellular Space::Cytoplasm::Cytoplasmic Structures::Organelles::Mitochondria [ANATOMY] ,Metabolisme, Errors congènits del ,Mitocondris - Malalties ,Molecular Biology ,Glycogen ,Cytoskeleton and mitochondrial network - Abstract
[Background]: McArdle disease is caused by myophosphorylase deficiency and results in complete inability for muscle glycogen breakdown. A hallmark of this condition is muscle oxidation impairment (e.g., low peak oxygen uptake (VO2peak)), a phenomenon traditionally attributed to reduced glycolytic flux and Krebs cycle anaplerosis. Here we hypothesized an additional role for muscle mitochondrial network alterations associated with massive intracellular glycogen accumulation. [Methods]: We analyzed in depth mitochondrial characteristics-content, biogenesis, ultrastructure-and network integrity in skeletal-muscle from McArdle/control mice and two patients. We also determined VO2peak in patients (both sexes, N = 145) and healthy controls (N = 133). [Results]: Besides corroborating very poor VO2peak values in patients and impairment in muscle glycolytic flux, we found that, in McArdle muscle: (a) damaged fibers are likely those with a higher mitochondrial and glycogen content, which show major disruption of the three main cytoskeleton components-actin microfilaments, microtubules and intermediate filaments-thereby contributing to mitochondrial network disruption in skeletal muscle fibers; (b) there was an altered subcellular localization of mitochondrial fission/fusion proteins and of the sarcoplasmic reticulum protein calsequestrin-with subsequent alteration in mitochondrial dynamics/function; impairment in mitochondrial content/biogenesis; and (c) several OXPHOS-related complex proteins/activities were also affected. [Conclusions]: In McArdle disease, severe muscle oxidative capacity impairment could also be explained by a disruption of the mitochondrial network, at least in those fibers with a higher capacity for glycogen accumulation. Our findings might pave the way for future research addressing the potential involvement of mitochondrial network alterations in the pathophysiology of other glycogenoses., The present study was funded by grants received from the Fondo de Investigaciones Sanitarias (FIS, PI17/02052, PI18/00139, PI19/01313, and PI20/00645) and cofunded by ‘Fondos FEDER’. Gisela Nogales-Gadea and Carmen Fiuza-Luces are supported by the Miguel Servet research contracts (ISCIII CD14/00032 and CP18/00034, respectively and cofounded by Fondos FEDER′). Research by Pedro L. Valenzuela is funded by a postdoctoral contract granted by Instituto de Salud Carlos III (Sara Borrell, CD21/00138). Monica Villarreal Salazar is supported by the Mexican National Council for Science and Technology (CONACYT).
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- 2022
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32. Exercise against nonsmall-cell lung carcinoma: novel insights.
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Plaza-Florido A, Fiuza-Luces C, and Lucia A
- Abstract
The mechanisms underlying the potential 'anticancer' effects of exercise remain poorly understood. Luo et al. recently identified an exercise-induced, muscle-derived extracellular vesicle (EV)-associated miR, miR-29a-3p, as a key player in the potential benefits of exercise against nonsmall-cell lung carcinoma (NSCLC), including extracellular matrix (ECM) inhibition and improved antitumoral immune responses., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
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- 2024
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33. Exercise and tumor proteome: insights from a neuroblastoma model.
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Plaza-Florido A, Gálvez BG, López JA, Santos-Lozano A, Zazo S, Rincón-Castanedo C, Martín-Ruiz A, Lumbreras J, Terron-Camero LC, López-Soto A, Andrés-León E, González-Murillo Á, Rojo F, Ramírez M, Lucia A, and Fiuza-Luces C
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- Animals, Mice, Male, Disease Models, Animal, Tandem Mass Spectrometry, Chromatography, Liquid, Proteomics methods, Neuroblastoma metabolism, Physical Conditioning, Animal physiology, Proteome metabolism, Protein Interaction Maps
- Abstract
The impact of exercise on pediatric tumor biology is essentially unknown. We explored the effects of regular exercise on tumor proteome profile (as assessed with liquid chromatography with tandem mass spectrometry) in a mouse model of one of the most aggressive childhood malignancies, high-risk neuroblastoma (HR-NB). Tumor samples of 14 male mice (aged 6-8 wk) that were randomly allocated into an exercise (5-wk combined aerobic and resistance training) or nonexercise control group (6 and 8 mice/group, respectively) were analyzed. The Search Tool for the Retrieval of Interacting Genes/Proteins database was used to generate a protein-protein interaction (PPI) network and enrichment analyses. The Systems Biology Triangle (SBT) algorithm was applied for analyses at the functional category level. Tumors of exercised mice showed a higher and lower abundance of 101 and 150 proteins, respectively, than controls [false discovery rate (FDR) < 0.05]. These proteins were enriched in metabolic pathways, amino acid metabolism, regulation of hormone levels, and peroxisome proliferator-activated receptor signaling (FDR < 0.05). The SBT algorithm indicated that 184 and 126 categories showed a lower and higher abundance, respectively, in the tumors of exercised mice (FDR < 0.01). Categories with lower abundance were involved in energy production, whereas those with higher abundance were related to transcription/translation, apoptosis, and tumor suppression. Regular exercise altered the abundance of hundreds of intratumoral proteins and molecular pathways, particularly those involved in energy metabolism, apoptosis, and tumor suppression. These findings provide preliminary evidence of the molecular mechanisms underlying the potential effects of exercise in HR-NB. NEW & NOTEWORTHY We used liquid chromatography with tandem mass spectrometry to explore the impact of a 5-wk exercise intervention on the tumor proteome profile in a mouse model of one of the most aggressive childhood malignancies, high-risk neuroblastoma. Exercise altered the abundance of hundreds of proteins and pathways, particularly those involved in energy metabolism and tumor suppression. These molecular changes could mediate, at least partly, the potential antitumorigenic effects of exercise.
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- 2024
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34. What time of the day should I exercise?
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Valenzuela PL, Santos-Lozano A, Fiuza-Luces C, and Lucia A
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- 2024
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35. Aerobic capacity and muscle proteome: Insights from a mouse model.
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Plaza-Florido A, Santos-Lozano A, López-Ortiz S, Gálvez BG, Arenas J, Martín MA, Valenzuela PL, Pinós T, Lucia A, and Fiuza-Luces C
- Abstract
We explored the association between aerobic capacity (AC) and the skeletal muscle proteome of McArdle (n = 10) and wild-type (n = 8) mice, as models of intrinsically 'low' and 'normal' AC, respectively. AC was determined as total distance achieved in treadmill running until exhaustion. The quadriceps muscle proteome was studied using liquid chromatography with tandem mass spectrometry, with the Search Tool for the Retrieval of Interacting Genes/Proteins database used to generate protein-protein interaction (PPI) networks and enrichment analyses. AC was significantly associated (P-values ranging from 0.0002 to 0.049) with 73 (McArdle) and 61 (wild-type) proteins (r-values from -0.90 to 0.94). These proteins were connected in PPI networks that enriched biological processes involved in skeletal muscle structure/function in both groups (false discovery rate <0.05). In McArdle mice, the proteins associated with AC were involved in skeletal muscle fibre differentiation/development, lipid oxidation, mitochondrial function and calcium homeostasis, whereas in wild-type animals AC-associated proteins were related to cytoskeleton structure (intermediate filaments), cell cycle regulation and endocytic trafficking. Two proteins (WEE2, THYG) were associated with AC (negatively and positively, respectively) in both groups. Only 14 of the 132 proteins (∼11%) associated with AC in McArdle or wild-type mice were also associated with those previously reported to be modified by aerobic training in these mice, providing preliminary evidence for a large divergence in the muscle proteome signature linked to aerobic training or AC, irrespective of AC (intrinsically low or normal) levels. Our findings might help to gain insight into the molecular mechanisms underlying AC at the muscle tissue level., (© 2024 The Author(s). Experimental Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society.)
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- 2024
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36. Exerkine response to acute exercise: Still much to discover.
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Valenzuela PL, Rivas-Baeza B, Fiuza-Luces C, and Lucia A
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- Humans, Muscle, Skeletal physiology, Exercise physiology
- Abstract
Competing Interests: Competing interests The authors declare that they have no competing interests.
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- 2024
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37. Can exercise kill tumors?
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Plaza-Florido A, Santos-Lozano A, Yanguas-Casás N, Pinós T, Fiuza-Luces C, and Lucia A
- Abstract
Competing Interests: Declaration of competing interest The authors declare that they have no competing interests.
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- 2024
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38. Anticancer effects of exercise: Insights from single-cell analysis.
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Plaza-Florido A, Lucia A, Radom-Aizik S, and Fiuza-Luces C
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- Single-Cell Analysis, Humans, Animals, Exercise standards, Neoplasms therapy
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- 2024
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39. Exercise benefits meet the esophagus.
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Santos-Lozano A, Valenzuela PL, Fiuza-Luces C, and Lucia A
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- Humans, Exercise physiology, Esophagus
- Abstract
Competing Interests: Competing interests The authors declare that they have no competing interests.
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- 2024
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40. Exercise Intolerance in McArdle Disease: A Role for Cardiac Impairment? A Preliminary Study in Humans and Mice.
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Santos-Lozano A, Boraita A, Valenzuela PL, Santalla A, Villarreal-Salazar M, Bustos A, Brea-Alejo L, Barranco-Gil D, Millán-Parlanti D, López-Ortiz S, Peñín-Grandes S, Orellana JN, Fiuza-Luces C, Gálvez BG, García-Fernández MÁ, Pinós T, and Lucia A
- Abstract
Introduction: Whether cardiac impairment can be fully discarded in McArdle disease-the paradigm of 'exercise intolerance', caused by inherited deficiency of the skeletal muscle-specific glycogen phosphorylase isoform ('myophosphorylase')-remains to be determined., Methods: Eight patients with McArdle disease and seven age/sex-matched controls performed a 15-minute moderate, constant-load cycle-ergometer exercise bout followed by a maximal ramp test. Electrocardiographic and two-dimensional transthoracic (for cardiac dimension's assessment) and speckle tracking [for left-ventricle global longitudinal (GLS) assessments] echocardiographic evaluations were performed at baseline. Electrocardiographic and GLS assessments were also performed during constant-load exercise and immediately upon maximal exertion. Four human heart biopsies were obtained in individuals without McArdle disease, and in-depth histological/molecular analyses were performed in McArdle and wild-type mouse hearts., Results: Exercise intolerance was confirmed in patients ('second wind' during constant-load exercise, -55% peak power output vs controls). As opposed to controls, patients showed a decrease in GLS during constant-load exercise, especially upon second wind occurrence, but with no other between-group difference in cardiac structure/function. Human cardiac biopsies showed that all three glycogen phosphorylase-myophosphorylase, but also liver and especially brain-isoforms are expressed in the normal adult heart, thereby theoretically compensating for eventual myophosphorylase deficiency. No overall histological (including glycogen depots), cytoskeleton, metabolic or mitochondrial (morphology/network/distribution) differences were found between McArdle and wild-type mouse hearts, except for lower levels of pyruvate kinase M2 and translocase of outer membrane 20 kDa subunit in the former., Conclusions: This study provides preliminary evidence that cardiac structure and function seem to be preserved in patients with McArdle disease. However, the role for an impaired cardiac contractility associated with the second wind phenomenon should be further explored., Competing Interests: Conflicts of Interest and Funding Source: The authors declare no conflicts of interest. Research by PLV is supported by a Sara Borrell postdoctoral contract granted by Instituto de Salud Carlos III (CD21/00138). TP is funded by the Spanish Ministry of Economy and Competitiveness and Fondos Feder (grant PI22/00201). AL and DBG are funded by the Spanish Ministry of Economy and Competitiveness and Fondos Feder (PI15/00558, and PI18/00139, respectively)., (Copyright © 2024 by the American College of Sports Medicine.)
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- 2024
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41. The effect of physical exercise on anticancer immunity.
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Fiuza-Luces C, Valenzuela PL, Gálvez BG, Ramírez M, López-Soto A, Simpson RJ, and Lucia A
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- Animals, Humans, Immune System, Exercise, Neoplasms therapy
- Abstract
Regular physical activity is associated with lower cancer incidence and mortality, as well as with a lower rate of tumour recurrence. The epidemiological evidence is supported by preclinical studies in animal models showing that regular exercise delays the progression of cancer, including highly aggressive malignancies. Although the mechanisms underlying the antitumorigenic effects of exercise remain to be defined, an improvement in cancer immunosurveillance is likely important, with different immune cell subtypes stimulated by exercise to infiltrate tumours. There is also evidence that immune cells from blood collected after an exercise bout could be used as adoptive cell therapy for cancer. In this Perspective, we address the importance of muscular activity for maintaining a healthy immune system and discuss the effects of a single bout of exercise (that is, 'acute' exercise) and those of 'regular' exercise (that is, repeated bouts) on anticancer immunity, including tumour infiltrates. We also address the postulated mechanisms and the clinical implications of this emerging area of research., (© 2023. Springer Nature Limited.)
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- 2024
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42. Author Correction: The effect of physical exercise on anticancer immunity.
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Fiuza-Luces C, Valenzuela PL, Gálvez BG, Ramírez M, López-Soto A, Simpson RJ, and Lucia A
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- 2024
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43. Exercise is also medicine for iron homeostasis.
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Plaza-Florido A, Lucia A, and Fiuza-Luces C
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- Humans, Homeostasis, Iron, Exercise, Exercise Therapy
- Abstract
High-intensity interval training (HIIT) is gaining popularity as an effective exercise modality to improve cardiometabolic health. Combining high-throughput/sensitivity proteome analyses in subcutaneous adipose tissue with biochemical blood measures, Larsen et al. recently provided mechanistic insights into a potential beneficial role of this exercise modality on iron homeostasis at the whole-body level., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
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- 2024
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44. Exercise and quality of life in cancer.
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Fiuza-Luces C, Valenzuela PL, Santos-Lozano A, Ruiz-Casado A, and Lucia A
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- Humans, Exercise, Exercise Therapy, Quality of Life, Neoplasms therapy
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- 2023
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45. Pathophysiology of Cerebellar Degeneration in Mitochondrial Disorders: Insights from the Harlequin Mouse.
- Author
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Fernández de la Torre M, Fiuza-Luces C, Laine-Menéndez S, Delmiro A, Arenas J, Martín MÁ, Lucia A, and Morán M
- Subjects
- Mice, Male, Animals, Proteomics, Cerebellum metabolism, Neurodegenerative Diseases metabolism, Mitochondrial Diseases metabolism, Cerebellar Diseases
- Abstract
By means of a proteomic approach, we assessed the pathways involved in cerebellar neurodegeneration in a mouse model (Harlequin , Hq ) of mitochondrial disorder. A differential proteomic profile study (iTRAQ) was performed in cerebellum homogenates of male Hq and wild-type (WT) mice 8 weeks after the onset of clear symptoms of ataxia in the Hq mice (aged 5.2 ± 0.2 and 5.3 ± 0.1 months for WT and Hq , respectively), followed by a biochemical validation of the most relevant changes. Additional groups of 2-, 3- and 6-month-old WT and Hq mice were analyzed to assess the disease progression on the proteins altered in the proteomic study. The proteomic analysis showed that beyond the expected deregulation of oxidative phosphorylation, the cerebellum of Hq mice showed a marked astroglial activation together with alterations in Ca
2+ homeostasis and neurotransmission, with an up- and downregulation of GABAergic and glutamatergic neurotransmission, respectively, and the downregulation of cerebellar "long-term depression", a synaptic plasticity phenomenon that is a major player in the error-driven learning that occurs in the cerebellar cortex. Our study provides novel insights into the mechanisms associated with cerebellar degeneration in the Hq mouse model, including a complex deregulation of neuroinflammation, oxidative phosphorylation and glutamate, GABA and amino acids' metabolism.- Published
- 2023
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46. Exercise benefits in cardiovascular diseases: from mechanisms to clinical implementation.
- Author
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Valenzuela PL, Ruilope LM, Santos-Lozano A, Wilhelm M, Kränkel N, Fiuza-Luces C, and Lucia A
- Subjects
- Humans, Exercise, Heart, Inflammation, Risk Factors, Cardiovascular Diseases prevention & control, Cardiovascular Diseases epidemiology, Cardiovascular System
- Abstract
There is a pandemic of physical inactivity that appears to parallel the widespread prevalence of cardiovascular disease (CVD). Yet, regular physical activity (PA) and exercise can play an important role not only in primary cardiovascular prevention but also in secondary prevention. This review discusses some of the main cardiovascular effects of PA/exercise and the mechanisms involved, including a healthier metabolic milieu with attenuation of systemic chronic inflammation, as well as adaptations at the vascular (antiatherogenic effects) and heart tissue (myocardial regeneration and cardioprotection) levels. The current evidence for safe implementation of PA and exercise in patients with CVD is also summarized., Competing Interests: Conflict of interest All authors declare no conflict of interest for this contribution., (© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.)
- Published
- 2023
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47. Validation and Determination of Physical Activity Intensity GT3X+ Cut-Points in Children and Adolescents with Physical Disabilities: Preliminary Results in a Cerebral Palsy Population.
- Author
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Matey-Rodríguez C, López-Ortiz S, Peñín-Grandes S, Pinto-Fraga J, Valenzuela PL, Pico M, Fiuza-Luces C, Lista S, Lucia A, and Santos-Lozano A
- Abstract
Background: Children and adolescents with disabilities engage in low levels of moderate-to-vigorous intensity physical activity (MVPA), which may create the onset of a sedentary lifestyle. In light of this, MVPA levels must be quantified with a valid tool such as accelerometry. This study aimed to: (i) analyze the accuracy of Evenson cut-points by estimating MVPA and sedentary behavior (SB) in children and adolescents with disabilities; (ii) define new equations to estimate energy expenditure (EE) with the GT3X+ accelerometer in this population and particularly in those with cerebral palsy (CP); (iii) define specific GT3X+ cut-points to estimate MVPA in those with CP., Methods: A total of 23 children and adolescents with disabilities (10 ± 3 years; 44%females) participated in the study. GT3X+-counts and oxygen uptake (VO
2 ) were measured in four laboratory walking conditions., Results: (i) Evenson cut-points were accurate; (ii) new equations were defined to effectively predict EE; (iii) specific GT3X+ cut-points (VM ≥ 702 counts·min-1 ; Y-Axis ≥ 360 counts·min-1 ) were defined for estimating MVPA levels in children and adolescents with CP., Conclusions: The use of specific cut-points for ActiGraph GT3X+ seems to be accurate to estimate MVPA levels in children and adolescents with disabilities and, particularly, in those with CP, at least in laboratory conditions.- Published
- 2023
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48. Physical Exercise and the Hallmarks of Breast Cancer: A Narrative Review.
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García-Chico C, López-Ortiz S, Peñín-Grandes S, Pinto-Fraga J, Valenzuela PL, Emanuele E, Ceci C, Graziani G, Fiuza-Luces C, Lista S, Lucia A, and Santos-Lozano A
- Abstract
Growing evidence suggests that, among the different molecular/cellular pathophysiological mechanisms associated with cancer, there are 14 hallmarks that play a major role, including: (i) sustaining proliferative signaling, (ii) evading growth suppressors, (iii) activating invasion and metastasis, (iv) enabling replicative immortality, (v) inducing angiogenesis, (vi) resisting cell death, (vii) reprogramming energy metabolism, (viii) evading immune destruction, (ix) genome instability and mutations, (x) tumor-promoting inflammation, (xi) unlocking phenotypic plasticity, (xii) nonmutational epigenetic reprogramming, (xiii) polymorphic microbiomes, and (xiv) senescent cells. These hallmarks are also associated with the development of breast cancer, which represents the most prevalent tumor type in the world. The present narrative review aims to describe, for the first time, the effects of physical activity/exercise on these hallmarks. In summary, an active lifestyle, and particularly regular physical exercise, provides beneficial effects on all major hallmarks associated with breast cancer, and might therefore help to counteract the progression of the disease or its associated burden.
- Published
- 2023
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49. Combined exercise intervention in a mouse model of high-risk neuroblastoma: effects on physical, immune, tumor and clinical outcomes.
- Author
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Rincón-Castanedo C, Martín-Ruiz A, Zazo S, Luis Huertas AL, Valenzuela PL, Morán M, Fleck SJ, Santos-Lozano A, Ramírez M, Rojo F, Lucia A, González-Murillo Á, and Fiuza-Luces C
- Subjects
- Male, Mice, Animals, Humans, Vascular Endothelial Growth Factor A, Muscle Strength physiology, Exercise Therapy, Tumor Microenvironment, Neuroblastoma therapy, Cardiorespiratory Fitness
- Abstract
Background: Exercise might exert anti-tumoral effects in adult cancers but this question remains open in pediatric tumors, which frequently show a different biology compared to adult malignancies. We studied the effects of an exercise intervention on physical function, immune variables and tumoral response in a preclinical model of a highly aggressive pediatric cancer, high-risk neuroblastoma (HR-NB)., Methods: 6-8-week-old male mice with orthotopically-induced HR-NB were assigned to a control (N = 13) or exercise (5-week combined [aerobic+resistance]) group (N = 17). Outcomes included physical function (cardiorespiratory fitness [CRF] and muscle strength), as well as related muscle molecular indicators, blood and tumor immune cell and molecular variables, tumor progression, clinical severity, and survival., Results: Exercise attenuated CRF decline (p=0.029 for the group-by-time interaction effect), which was accompanied by higher muscle levels of oxidative capacity (citrate synthase and respiratory chain complexes III, IV and V) and an indicator of antioxidant defense (glutathione reductase) in the intervention arm (all p≤0.001), as well as by higher levels of apoptosis (caspase-3, p=0.029) and angiogenesis (vascular endothelial growth factor receptor-2, p=0.012). The proportion of 'hot-like' (i.e., with viable immune infiltrates in flow cytometry analyses) tumors tended to be higher (p=0.0789) in the exercise group (76.9%, vs. 33.3% in control mice). Exercise also promoted greater total immune (p=0.045) and myeloid cell (p=0.049) infiltration within the 'hot' tumors, with a higher proportion of two myeloid cell subsets (CD11C+ [dendritic] cells [p=0.049] and M2-like tumor-associated macrophages [p=0.028]), yet with no significant changes in lymphoid infiltrates or in cirulating immune cells or chemokines/cytokines. No training effect was found either for muscle strength or anabolic status, cancer progression (tumor weight and metastasis, tumor microenvironment), clinical severity, or survival., Conclusions: Combined exercise appears as an effective strategy for attenuating physical function decline in a mouse model of HR-NB, also exerting some potential immune benefits within the tumor, which seem overall different from those previously reported in adult cancers., (Copyright © 2023 International Society of Exercise and Immunology. All rights reserved.)
- Published
- 2023
50. Childhood cancer: exercise is medicine.
- Author
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Fiuza-Luces C, Valenzuela PL, Morales JS, and Lucia A
- Subjects
- Child, Humans, Exercise, Neoplasms therapy, Cancer Survivors
- Abstract
Competing Interests: We declare no competing interests. Research by AL and CF-L is funded by the Wereld Kanker Onderzoek Fonds as part of the World Cancer Research Fund International grant programme.
- Published
- 2023
- Full Text
- View/download PDF
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